反応 #595396

ord-028016107ac5438fb8dc40d6d7facb0b

反応方程式

Cc1ccc(NN)cc1.Cl
p-tolylhydrazine hydrochloride
CCOC(=O)N1CCC(=O)CC1
1-carbethoxy-4-piperidone
CCOC(=O)N1CCc2[nH]c3ccc(C)cc3c2C1
desired product
収率 86.0%
CCOC(=O)N1CCc2[nH]c3ccc(C)cc3c2C1
Ethyl 8-Methyl-3,4-dihydro-1H-pyrido[4,3-b]indole-2(5H)-carboxylate
収率 86.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度heated
  2. 2
    温度to reflux for 2 hours
  3. 3
    その他The reaction mixture was removed
  4. 4
    温度from heat
  5. 5
    ろ過The resulting mixture was filtered
  6. 6
    洗浄washed with 50% aqueous EtOH

実験手順

Following a literature procedure (Harbert et al., J. Med. Chem. 1980, 23, 635-643) p-tolylhydrazine hydrochloride (0.500 g, 3.15 mmol) and 1-carbethoxy-4-piperidone (0.18 mL, 1.17 mmol) were suspended in EtOH (0.880 mL) and heated to reflux for 2 hours. The reaction mixture was removed from heat and allowed to stand overnight at ambient temperature. The resulting mixture was filtered and washed with 50% aqueous EtOH to afford the desired product as a beige powder (259 mg, 86%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09095572B2uspto-grants-2015_08